The Significance and Clinical Outcome of Lymphocytic Duodenosis in Children: Mayo Clinic Experience and Systematic Review.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 15 9 2020
medline: 22 6 2021
entrez: 14 9 2020
Statut: ppublish

Résumé

Lymphocytic duodenosis (LD) defined as increased intraepithelial lymphocytes >25 intraepithelial lymphocytes (IELs) per 100 epithelial cells with normal villous architecture is associated with many gastrointestinal (GI) disorders. We aim to assess the rate and outcome of LD in children and perform a systematic review. We reviewed all children (<18 years) who underwent esophagogastroduodenoscopy (EGD) with duodenal biopsy between January 2000 and June 2019 to identify LD cases and control group. Demographics, clinical, and pathologic information were reviewed and recorded. A systematic review including our findings was performed. During the study period 12,744 children underwent an EGD with biopsies. Of those, we identified 426 children with LD (3%) and 474 controls. The median age in years was 10.7 and 12.6 and there were 254 (60%) and 278 (59%) girls in the LD and control group, respectively. The most common presenting symptoms in both groups were abdominal pain (52%), gastroesophageal acid reflux disease (18%), diarrhea (16%), and vomiting (12%). Diarrhea (21% vs 12%, P < 0.001) and constipation (2% vs 0.4%, P = 0.021) were statistically different between the LD and control group, respectively. Median follow-up (range) is 3.6 (0.0, 190.9) and 3.1 (0.0, 194.2) in the LD and control group, respectively. CD (5% vs 0%, P < 0.001), Crohn disease (9% vs 3%, P = 0.003) and Helicobacter pylori gastritis (3% vs 1%, P = 0.021) were more common in the LD group. The Rate of LD in children is similar to reported rate in adults. In the absence of Crohn disease, CD or H. Pylori, LD seems to be a benign and transient histologic finding in children.

Sections du résumé

BACKGROUND
Lymphocytic duodenosis (LD) defined as increased intraepithelial lymphocytes >25 intraepithelial lymphocytes (IELs) per 100 epithelial cells with normal villous architecture is associated with many gastrointestinal (GI) disorders. We aim to assess the rate and outcome of LD in children and perform a systematic review.
METHOD
We reviewed all children (<18 years) who underwent esophagogastroduodenoscopy (EGD) with duodenal biopsy between January 2000 and June 2019 to identify LD cases and control group. Demographics, clinical, and pathologic information were reviewed and recorded. A systematic review including our findings was performed.
RESULTS
During the study period 12,744 children underwent an EGD with biopsies. Of those, we identified 426 children with LD (3%) and 474 controls. The median age in years was 10.7 and 12.6 and there were 254 (60%) and 278 (59%) girls in the LD and control group, respectively. The most common presenting symptoms in both groups were abdominal pain (52%), gastroesophageal acid reflux disease (18%), diarrhea (16%), and vomiting (12%). Diarrhea (21% vs 12%, P < 0.001) and constipation (2% vs 0.4%, P = 0.021) were statistically different between the LD and control group, respectively. Median follow-up (range) is 3.6 (0.0, 190.9) and 3.1 (0.0, 194.2) in the LD and control group, respectively. CD (5% vs 0%, P < 0.001), Crohn disease (9% vs 3%, P = 0.003) and Helicobacter pylori gastritis (3% vs 1%, P = 0.021) were more common in the LD group.
CONCLUSIONS
The Rate of LD in children is similar to reported rate in adults. In the absence of Crohn disease, CD or H. Pylori, LD seems to be a benign and transient histologic finding in children.

Identifiants

pubmed: 32925553
pii: 00005176-202102000-00022
doi: 10.1097/MPG.0000000000002942
doi:

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

288-293

Informations de copyright

Copyright © 2020 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Références

Hammer STG, Greenson JK. The clinical significance of duodenal lymphocytosis with normal villus architecture. Arch Pathol Lab Med 2013; 137:1216–1219.
MacDonald TT, Bajaj-Elliott M, Pender SL. T cells orchestrate intestinal mucosal shape and integrity. Immunol Today 1999; 20:505–510.
Ferguson A, Murray D. Quantitation of intraepithelial lymphocytes in human jejunum. Gut 1971; 12:988–994.
Hayat M, Cairns A, Dixon MF, et al. Quantitation of intraepithelial lymphocytes in human duodenum: what is normal? J Clin Pathol 2002; 55:393–394.
Friedt M, Welsch S. An update on pediatric endoscopy. Eur J Med Res 2013; 18:24.
Yousef MM, Yantiss RK, Baker SP, et al. Duodenal intraepithelial lymphocytes in inflammatory disorders of the esophagus and stomach. Clin Gastroenterol Hepatol 2006; 4:631–634.
Melin-Aldana H, Arva NC. Significance of mild isolated increase in intraepithelial lymphocytes in pediatric duodenal biopsies. Pediatr Dev Pathol 2015; 18:e45.
Kakar S, Nehra V, Murray JA, et al. Significance of intraepithelial lymphocytosis in small bowel biopsy samples with normal mucosal architecture. Am J Gastroenterol 2003; 98:2027–2033.
Veress B, Franzén L, Bodin L, et al. Duodenal intraepithelial lymphocyte-count revisited. Scand J Gastroenterol 2004; 39:138–144.
Dickson BC, Streutker CJ, Chetty R. Coeliac disease: an update for pathologists. J Clin Pathol 2006; 59:1008–1016.
Mavromichalis J, Zannos-Mariolea L, Nicolaidou M, et al. Evaluation of the intraepithelial lymphocyte count in the jejunum in childhood enteropathies. Gut 1976; 17:600–603.
Taylor CJ. Predictive value of intraepithelial lymphocyte counts in childhood coeliac disease. J Pediatr Gastroenterol Nutr 1988; 7:532–536.
Klemola T. Immunohistochemical findings in the intestine of IgA-deficient persons: number of intraepithelial T lymphocytes is increased. J Pediatr Gastroenterol Nutr 1988; 7:537–543.
Montgomery RD, Shearer AC. The cell population of the upper jejunal mucosa in tropical sprue and postinfective malabsorption. Gut 1974; 15:387–391.
Ferguson A, McClure JP, Townley RR. Intraepithelial lymphocyte counts in small intestinal biopsies from children with diarrhoea. Acta Paediatr Scand 1976; 65:541–546.
Shmidt E, Smyrk TC, Faubion WA, et al. Duodenal intraepithelial lymphocytosis with normal villous architecture in pediatric patients: Mayo Clinic experience 2000-2009. J Pediatr Gastroenterol Nutr 2013; 56:51–55.
Patterson ER, Shmidt E, Oxentenko AS, et al. Normal villous architecture with increased intraepithelial lymphocytes: a duodenal manifestation of Crohn disease. Am J Clin Pathol 2015; 143:445–450.
Walker MM, Murray JA, Ronkainen J, et al. Detection of celiac disease and lymphocytic enteropathy by parallel serology and histopathology in a population-based study. Gastroenterology 2010; 139:112–119.
Aziz I, Evans KE, Hopper AD, et al. A systematic approach identifying the causes of duodenal intraepithelial lymphocytosis. Gut 2010; 59: (Suppl 1): A33.
Yu YH, Han DS, Choi EY, et al. Is use of PPIs related to increased intraepithelial lymphocytes in the colon? Digest Dis Sci 2012; 57:2669–2674.
Sollid LM, Markussen G, Ek J, et al. Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer. J Exp Med 1989; 169:345–350.
Murdock AM, Johnston SD. Diagnostic criteria for coeliac disease: time for change? Eur J Gastroenterol Hepatol 2005; 17:41–43.
Kårhus LL, Markussen G, Ek J, et al. The distribution of HLA DQ2 and DQ8 haplotypes and their association with health indicators in a general Danish population. United European Gastroenterology Journal 2018; 6:866–878.
Kurppa K, Thuesen BH, Skaaby T, et al. Diagnosing mild enteropathy celiac disease: a randomized, controlled clinical study. Gastroenterology 2009; 136:816–823.
Michaelsson G, Kraaz W, Gerdén B, et al. Increased lymphocyte infiltration in duodenal mucosa from patients with psoriasis and serum IgA antibodies to gliadin. Br J Dermatol 1995; 133:896–904.
Leffler D, Schuppan D, Pallav K, et al. Kinetics of the histological, serological and symptomatic responses to gluten challenge in adults with coeliac disease. Gut 2013; 62:996–1004.

Auteurs

Janaki Devara (J)

Division of Pediatric Gastroenterology, Hepatology and Nutrition.

Mouaz Alsawas (M)

Mayo Clinic Evidence-based Practice Center.

Joseph J Larson (JJ)

Department of Biomedical Statistics and informatics.

Taofic Mounajjed (T)

Department of Pathology, Mayo Clinic, Rochester, MN.

Joseph A Murray (JA)

Division of Gastroenterology and Hepatology.

Imad Absah (I)

Division of Pediatric Gastroenterology, Hepatology and Nutrition.
Division of Gastroenterology and Hepatology.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH